RS11986414 Unknown gene

Other Chr 8:1798784
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What This Variant Does
"Genome-wide association study of N370S homozygous Gaucher disease reveals the candidacy of CLN8 gene as a genetic modifier contributing to extreme phenotypic variation"
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
Gaucher disease severity A OR: 3.72 1E-6 PubMed
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